SNP Report

Basic Info

Name	rs9946695 dbSNP Ensembl
Location	chr18:9196530 - 9196530(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.307308
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000585234); intron_variant(ENST00000262126, ENST00000400020, ENST00000540578, ENST00000546007, ENST00000578850, ENST00000581635, ENST00000581758); NMD_transcript_variant(ENST00000581635); non_coding_transcript_variant(ENST00000540578, ENST00000578850, ENST00000581758)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ANKRD12	ankyrin repeat domain 12	18p11.22	Mapped by Literature SNP

SNPs in LD with rs9946695 (count: 0) View in gBrowse (chr18:9196530..9196530 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)